A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223788



Internal ID22367456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15415549..15420687hg38UCSC Ensembl
chr12:15568483..15573621hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg385139
hg195139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360384
SamplesNA19238
Known GenesPTPRO
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223788
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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